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NCT Number: NCT05825612

EPIRUS FH Reverse Cascade Screening

Familial hypercholesterolemia (FH) is the most common inherited metabolic disorder resulting in marked elevations in low-density lipoprotein cholesterol (LDL-C). If left untreated, lifelong exposure to elevated LDL-C leads to a substantially increased risk of premature cardiovascular disease as compared to the general population. Although FH adverse cardiovascular outcomes are potentially preventable through early identification of FH individuals and initiation of effective treatment, available evidence shows that FH is under-diagnosed and under-treated.

Childhood is the optimal period for FH screening, because due to minimal dietary and hormonal influences, LDL-C levels reflect predominantly the genetic component in children and are well suited to discriminate FH from other causes of elevated LDL-C. If FH remains untreated in this latent stage of the disease, individuals show a 10-fold increase of cardiovascular risk during early and middle adulthood. In this context, an effective approach for detecting FH would be a screening during childhood or in young adolescents in combination with reverse cascade screening of first-degree relatives of FH individuals.

EPIRUS-FH registry is a model program of reverse cascade screening for FH in children and adolescents in Northwest Greece that aims to increase public and physician awareness, strengthen the national registry of familial hypercholesterolemia (HELLAS-FH) and constitute the core for a national FH registry in children and adolescents in Greece.

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Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • LDL-C >160 mg/dL on two seperate measurements 3 months apart
  • LDL-C >130 mg/dL + family history of premature coronary artery disease or hypercholesterolemia in one parent
  • Children and adolescents on cholesterol-lowering medication

Exclusion criteria

  • Refusal to sign the consent form and disagreement with the terms of participation.
  • Any clinically significant disorder recognized at the time of the preliminary assessment, which in the judgment of the investigator would disqualify patient's participation in the study.

Treatment and study plan

Primary outcomes

  1. Diagnosis of Familial Hypercholesterolemia

    Time frame: Baseline

    Type of FH (Heterozygous FH, Homozygous FH). In the case of genetic diagnosis, what gene was affected (LDL receptor, Apolipoprotein B, PCSK9, LDLRAP1, other to be specified).

    Age at diagnosis of FH.

Study contacts

Contact information is provided by the study sponsor or research team.

Fotios Barkas

CONTACT

[email protected]

+306936636376

Haralampos Milionis

CONTACT

[email protected]

+302651099736

Sponsors and collaborators

Lead sponsor

Hellenic Atherosclerosis Society

Other

Registry information

Official study title

Reverse Cascade Screening for Familial Hypercholesterolemia in Children and Adolescents in Northwest Greece

Important dates

Study start
2023
Primary completion
2033
Study completion
2033
First posted
Apr 24, 2023
Registry last updated
Apr 24, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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